Allele Registry

Canonical Allele Identifier: PA2825652217

Gene: GSN HGNC NCBI

ClinVar RCV:

RCV000017565

RCV003556034

ClinVar Variation:

16181

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121139.1:p.Asp174Tyr	CA250654 NM_001127667.2:c.520G>T